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Water → (5-Phenyl-1,2-oxazol-3-yl)methanol

HRID 384105
ノート
印刷プレビュー

反応式

HRID 384105 の反応式
[C:1]1([C:7]2[O:11][N:10]=[C:9]([C:12](O)=[O:13])[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O.C(=O)([O-])O.[Na+]>O1CCCC1.B.O1CCCC1>[C:1]1([C:7]2[O:11][N:10]=[C:9]([CH2:12][OH:13])[CH:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 1519165-Phenyl-3-isoxazolecarboxylic acidHCID 516892Sodium Bicarbonate

生成物 1

HCID 1481082(5-Phenyl-1,2-oxazol-3-yl)methanol

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 2723981Borane;tetrahydrofuran溶媒

反応条件

温度
80 °C

実験手順

To a solution of 5-phenylisoxazol-3-carboxylic acid (551 mg) in tetrahydrofuran (15 ml), 3.7 ml of borane-tetrahydrofuran complex (1.17M tetrahydrofuran solution) was added, and the reaction solution was stirred at 80° C. for 10 hours. Water and a saturated aqueous sodium hydrogen carbonate solution were added to the reaction solution, and the mixture was extracted with chloroform and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: ethyl acetate/hexane (10:90-50:50)) to afford the title compound as a white solid.

後処理

  1. extractionthe mixture was extracted with chloroform
  2. dry with materialdried over anhydrous sodium sulfate
  3. distillationThe solvent was distilled off under reduced pressure
  4. customthe residue obtained
  5. customwas purified by silica gel column chromatography (eluent: ethyl acetate/hexane (10:90-50:50))

出典と根拠

ORDレコード
ord-a98cd7beb9034572938093d25c166f48
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367708B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート